I Keser - Concepedia

Author

I Keser

Akdeniz University

Also Known As

I Keser, I. KESER, I. Keser, Keser, Ibrahim, İBRAHİM KESER, İbrahim Keser

Publications

674

Citations

H-Index

Concepts

All Affiliations

Akdeniz University Antalya IVF

About

I Keser is an author at Akdeniz University specializing in medicine, genetics, and monogenic disorders.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	570
2	Natural Sciences	1	1	28
3	Public Health	1	1	11
4	Allergy	1	1	425
5	Biochemistry	1	1	28

I Keser

Publications

616

Citations

H-Index

Page 1

	Year	Citations
The Arg753Gln polymorphism of the human Toll-like receptor 2 gene in tuberculosis disease A.C. Ogus, Burçak Yoldaş, Taha Reşid Özdemir, European Respiratory Journal Innate Immune SystemImmunologyGenetic EpidemiologyHuman PolymorphismInnate Immunity	2004	425
Normal phenotype with maternal isodisomy in a female with two isochromosomes: i(2p) and i(2q) Ahmet Karagüzel, Figen Celep, I Keser, PubMed ChromatinCytogeneticsGenetic DisorderGeneticsMaternal Isodisomy	1996	61
The Effect of MDR1 (ABCB1) Polymorphism on the Pharmacokinetic of Tacrolimus in Turkish Renal Transplant Recipients S. Halide Akbaş, Türker Bilgen, I Keser, Transplantation Proceedings UrologyKidney TransplantMedicineKidney TransplantationPharmacology	2006	45
Molecular Analysis of Beta-Thalassemia and Sickle Cell Anemia in Antalya I Keser, Ahter Dilşad Şanlioğlu, Esra Manguoğlu, Acta Haematologica BiologyAllelic VariantHaplotype DeterminationThalassemia UnitBiochemistry	2004	28
Two novel mutations in the 3′ untranslated region of the beta‐globin gene that are associated with the mild phenotype of beta thalassemia Türker Bilgen, Özden Altıok Clark, Zeynep Öztürk, International Journal of Laboratory Hematology	2012	26
Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridisation. M. Alkan, Gian Paolo Ramelli, Hans Hirsiger, PubMed CytogeneticsGeneticsPathologySitu HybridisationPresumptive Monosomy 21	2002	11
Molecular analysis of fragile X syndrome in Antalya Province I Keser, Şenay Haspolat, Şükran Taçoy, Indian Journal of Medical Sciences	2005	10
Frequencies of four genetic polymorphisms in the CYP1A2 gene in Turkish population Türker Bilgen, Özgür Tosun, Güven Lüleci, Russian Journal of Genetics	2008	10

Page 1